Results 41 to 50 of about 3,502,764 (202)

Clinical and genetic features of pediatric hereditary polyposis syndromes in Israel: A nationwide multicenter cohort

Journal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objectives Hereditary polyposis syndromes in children are rare, heterogeneous disorders associated with significant morbidity and long‐term risk of malignancy. Current data on their presentation, management, and outcomes in pediatric populations remain limited.
Shlomi Cohen, Tal Cozacov, Ilana Weintraub, Ron Shaoul, Oren Ledder, Dotan Yogev, Mordechai Slae, Ranya Egbarieh, Galina Ling, Anat Yerushalmy‐Feler   +9 more
wiley   +1 more source

Clinical presentation and endoscopic features of primary gastric Burkitt lymphoma in childhood, presenting as a protein-losing enteropathy: a case report

Journal of Medical Case Reports, 2009
Introduction Burkitt lymphoma and B cell lymphomas in childhood may arise in many atypical locations, which on rare occasions can include gastric mucosa.
Chieng Jenny Hui Chia, Garrett John, Ding Steven Leslie, Sullivan Michael   +3 more
doaj   +1 more source

Malnutrition and chyle leakage: A life‐threatening duo in heart transplantation post‐Fontan procedure

Clinical Case Reports, 2020
Protein‐losing enteropathy and chyle leakage may lead to severe malnutrition in heart transplantation for failing Fontan. Nutritional management may be challenging from defining nutrient needs to diagnosis of malnutrition enteropathy, and expertise is ...
Antonella Lezo, Enrico Aidala, Luca Deorsola, Maria Teresa Cascarano, Alberta Rizzo, Stefania Iannandrea, Licia Peruzzi, Federica Runfola, Carlo Pace Napoleone   +8 more
doaj   +1 more source

The genetic landscape of congenital diarrheas and very early onset inflammatory bowel disease in the Middle East

JPGN Reports, EarlyView.
Abstract Objectives Monogenic causes of congenital diarrheas and enteropathies (CoDE) and very early onset inflammatory bowel disease (VEOIBD) are mostly recessive and therefore more prevalent in populations with increased consanguinity rates. To assess the genetic basis of these disorders in a likely high‐prevalence population, we established a multi ...
Lily Gillette, Muna Al Safar, Ganeshwaran H. Mochida, Casey Johnson, Stephen Babcock, Klaus Schmitz‐Abe, Michael Field, Jessica Yang, Richelle Bearup, Ahmed Megahed, Mohammed Ezz El Regal Abbas, Tarek Baraket, Sherine Elziny, Ali Sobh, Gulin Eren, Fawaz AlRefaee, Rana Bitar, Mohamed Miqdady, Pankaj B. Agrawal, Scott B. Snapper, Jay R. Thiagarajah, Jodie Ouahed   +21 more
wiley   +1 more source

Protein-losing enteropathy associated with heart disease

, 2018
Protein-losing enteropathy is a rare complication of heart diseases associated with a chronic increase in systemic venous pressure. The most common cardiac cause of protein-losing enteropathy is found in patients after the Fontan operation.
Conall Morgan, Luc Mertens
core   +1 more source

Intestinal Lymphangiectasia Secondary to Neuroblastoma

Canadian Journal of Gastroenterology, 1994
An eight month-old infant presented with a 10-day history of vomiting and diarrhea, and a one-week history of swelling of the lower extremities. Laboratory evaluations revealed hypoproteinemia and lymphocytopenia due to protein-losing enteropathy ...
RM Reifen, PM Sherman
doaj   +1 more source

Reversal of surgical biliary diversion with ileal bile acid transport inhibitors: A new chapter in progressive familiar intrahepatic cholestasis type 1 management?

JPGN Reports, EarlyView.
Abstract Progressive Familial Intrahepatic Cholestasis type 1 (PFIC1) is a multisystem disorder. Although liver transplant (LT) resolves the hepatic disease, post‐LT complications may occur, including severe enteropathy and graft steatosis caused by impaired bile acids handling by the native intestine.
Teresa Botelho, Giulia Jannone, Roberto Tambucci, Catherine de Magnee, Isabelle Scheers, Etienne Sokal, Xavier Stephenne   +6 more
wiley   +1 more source

Cisterna Chyli Dilation Is a Risk Factor for Liver Nodules and Hepatocellular Carcinoma in Fontan‐Associated Liver Disease: Pathophysiological Role of Lymphatic Dysfunction

Hepatology Research, EarlyView.
ABSTRACT Aim In Fontan‐associated liver disease (FALD), chronic congestion often confounds conventional fibrosis markers, complicating surveillance for hepatocellular carcinoma (HCC). Although lymphatic dysfunction is fundamental to Fontan physiology, its contribution to hepatocarcinogenesis remains unclear.
Koji Imoto, Masatake Tanaka, Takeshi Goya, Yuuki Azuma, Tomonobu Hioki, Yusuke Morita, Keisuke Sakaguchi, Nobuhiro Fujita, Takamori Kakino, Ayako Ishikita, Kenichiro Yamamura, Ichiro Sakamoto, Kousei Ishigami, Kohtaro Abe, Yoshihiro Ogawa   +14 more
wiley   +1 more source

Case Report: Food Protein-Induced Protein Losing Enteropathy (FPIPLE) in Infancy

Frontiers in Nutrition, 2022
Food-protein induced protein-losing enteropathy (FPIPLE) is a mixed IgE and non-IgE food allergy in infants along with eosinophilic gastrointestinal (GI) diseases (EGID).
Gavriela Feketea, Gavriela Feketea, Alina Popp, Alina Popp, Daniela Marcela Ionescu, Daniela Marcela Ionescu, Elena Camelia Berghea, Elena Camelia Berghea   +7 more
doaj   +1 more source

Myofibroma: From protein losing enteropathy to liver tumor

Journal of Pediatric Surgery Case Reports, 2014
Myofibromas are rare fibrous tumors, which can be solitary (myofibroma) or multiple (myofibromatosis). They can be dermatological or visceral in origin.
Deepali Tewari, Virendra Tewari, Stuart Berezin, Michael Halata   +3 more
doaj   +1 more source